메뉴 건너뛰기




Volumn 72, Issue 2, 2007, Pages 327-340

Molecular interaction of a potent nonpeptide agonist with the chemokine receptor CCR8

Author keywords

[No Author keywords available]

Indexed keywords

1 [5 CHLORO 2 [2 [4 (4 FLUOROBENZYL) 2 METHYL 1 PIPERAZINYL] 2 OXOETHOXY]PHENYL]UREA; 2 [1 [3 (2 METHOXYPHENOXY)BENZYL] 4 HYDROXYPIPERIDIN 4 YL]BENZOIC ACID; 2 [2 [4 (3 PHENOXYBENZYL)PIPERAZIN 1 YL]ETHOXY]ETHANOL; 8 [3 (2 METHOXYPHENOXY)BENZYL] 1 PHENETHYL 1,3,8 TRIAZASPIRO[4.5]DECAN 4 ONE; ALANINE; CHEMOKINE RECEPTOR AGONIST; CHEMOKINE RECEPTOR CCR1; CHEMOKINE RECEPTOR CCR2; CHEMOKINE RECEPTOR CCR5; CHEMOKINE RECEPTOR CCR8; GLUTAMIC ACID; LMD 009; LMD 174; LMD 268; LMD 584; LMD 902; N ETHYL 2 4 METHOXYBENZENESULFONAMIDE; N [1 [3 (2 METHOXYPHENOXY)BENZYL]PIPERIDIN 4 YL] 1,2,3,4 TETRAHYDRO 2 OXOQUINOLINE 4 CARBOXAMIDE; N [1 [3 (2 METHOXYPHENOXY)BENZYL]PIPERIDIN 4 YL] 2 PHENYL 4 (PYRROLIDIN 1 YL)BUTANAMIDE; PHENYLALANINE; UNCLASSIFIED DRUG; ZK 756326;

EID: 34547177384     PISSN: 0026895X     EISSN: 15210111     Source Type: Journal    
DOI: 10.1124/mol.107.035543     Document Type: Article
Times cited : (50)

References (40)
  • 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
    • 77957055780 scopus 로고
    • Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G protein-coupled receptors
    • Sealfon SC ed, pp, Academic Press, New York
    • Ballesteros JA and Weinstein H (1995) Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G protein-coupled receptors, in Receptor Molecular Biology (Sealfon SC ed), pp 366-428, Academic Press, New York.
    • (1995) Receptor Molecular Biology , pp. 366-428
    • Ballesteros, J.A.1    Weinstein, H.2
  • 4
    • 12244267994 scopus 로고    scopus 로고
    • Binding of 2-aryl-4-(piperidin-1-yl)butanamines and 1,3,4-trisubstituted pyrrolidines to human CCR5: A molecular modeling-guided mutagenesis study of the binding pocket
    • Castonguay LA, Weng Y, Adolfsen W, Di Salvo J, Kilburn R, Caldwell CG, Daugherty BL, Finke PE, Hale JJ, Lynch CL, et al. (2003) Binding of 2-aryl-4-(piperidin-1-yl)butanamines and 1,3,4-trisubstituted pyrrolidines to human CCR5: a molecular modeling-guided mutagenesis study of the binding pocket. Biochemistry 42:1544-1550.
    • (2003) Biochemistry , vol.42 , pp. 1544-1550
    • Castonguay, L.A.1    Weng, Y.2    Adolfsen, W.3    Di Salvo, J.4    Kilburn, R.5    Caldwell, C.G.6    Daugherty, B.L.7    Finke, P.E.8    Hale, J.J.9    Lynch, C.L.10
  • 6
    • 0033618444 scopus 로고    scopus 로고
    • HHV8-encoded VMIP-I selectively engages chemokine receptor CCR8. Agonist and antagonist profiles of viral chemokines
    • Dairaghi DJ, Fan RA, McMaster BE, Hanley MR, and Schall TJ (1999) HHV8-encoded VMIP-I selectively engages chemokine receptor CCR8. Agonist and antagonist profiles of viral chemokines. J Biol Chem 274:21569- 21574.
    • (1999) J Biol Chem , vol.274 , pp. 21569-21574
    • Dairaghi, D.J.1    Fan, R.A.2    McMaster, B.E.3    Hanley, M.R.4    Schall, T.J.5
  • 7
    • 0032568510 scopus 로고    scopus 로고
    • Broad spectrum chemokine antagonistic activity of a human poxvirus chemokine homolog
    • Damon I, Murphy PM, and Moss B (1998) Broad spectrum chemokine antagonistic activity of a human poxvirus chemokine homolog. Proc Natl Acad Sci 95:6403-6407.
    • (1998) Proc Natl Acad Sci , vol.95 , pp. 6403-6407
    • Damon, I.1    Murphy, P.M.2    Moss, B.3
  • 8
    • 14244254079 scopus 로고    scopus 로고
    • Site-directed mutagenesis of CC chemokine receptor 1 reveals the mechanism of action of UCB 35625, a small molecule chemokine receptor antagonist
    • de Mendonça FL, da Fonseca PC, Phillips RM, Saldanha JW, Williams TJ, and Pease JE (2005) Site-directed mutagenesis of CC chemokine receptor 1 reveals the mechanism of action of UCB 35625, a small molecule chemokine receptor antagonist. J Biol Chem 280:4808-4816.
    • (2005) J Biol Chem , vol.280 , pp. 4808-4816
    • de Mendonça, F.L.1    da Fonseca, P.C.2    Phillips, R.M.3    Saldanha, J.W.4    Williams, T.J.5    Pease, J.E.6
  • 9
    • 0029907599 scopus 로고    scopus 로고
    • Requirement of rigid-body motion of transmembrane helices for light activation of rhodopsin
    • Farrens DL, Altenbach C, Yang K, Hubbell WL, and Khorana HG (1996) Requirement of rigid-body motion of transmembrane helices for light activation of rhodopsin. Science 274:768-770.
    • (1996) Science , vol.274 , pp. 768-770
    • Farrens, D.L.1    Altenbach, C.2    Yang, K.3    Hubbell, W.L.4    Khorana, H.G.5
  • 10
    • 0035260881 scopus 로고    scopus 로고
    • Chemokines and disease
    • Gerard C and Rollins BJ (2001) Chemokines and disease. Nat Immunol 2:108-115.
    • (2001) Nat Immunol , vol.2 , pp. 108-115
    • Gerard, C.1    Rollins, B.J.2
  • 11
    • 33646455298 scopus 로고    scopus 로고
    • Design, synthesis, and progress toward optimization of potent small molecule antagonists of CC chemokine receptor 8 (CCR8)
    • Ghosh S, Elder A, Guo J, Mani U, Patane M, Carson K, Ye Q, Bennett R, Chi S, Jenkins T, et al. (2006) Design, synthesis, and progress toward optimization of potent small molecule antagonists of CC chemokine receptor 8 (CCR8). J Med Chem 49:2669-2672.
    • (2006) J Med Chem , vol.49 , pp. 2669-2672
    • Ghosh, S.1    Elder, A.2    Guo, J.3    Mani, U.4    Patane, M.5    Carson, K.6    Ye, Q.7    Bennett, R.8    Chi, S.9    Jenkins, T.10
  • 15
    • 33747603675 scopus 로고    scopus 로고
    • Ghrelin receptor inverse agonists: Identification of an active peptide core and its interaction epitopes on the receptor
    • Holst B, Lang M, Brandt E, Bach A, Howard A, Frimurer TM, Beck-Sickinger A, and Schwartz TW (2006) Ghrelin receptor inverse agonists: identification of an active peptide core and its interaction epitopes on the receptor. Mol Pharmacol 70:936-946.
    • (2006) Mol Pharmacol , vol.70 , pp. 936-946
    • Holst, B.1    Lang, M.2    Brandt, E.3    Bach, A.4    Howard, A.5    Frimurer, T.M.6    Beck-Sickinger, A.7    Schwartz, T.W.8
  • 16
    • 0037396434 scopus 로고    scopus 로고
    • Development and evaluation of pharmacological agents targeting chemokine receptors
    • Horuk R (2003) Development and evaluation of pharmacological agents targeting chemokine receptors. Methods 29:369-375.
    • (2003) Methods , vol.29 , pp. 369-375
    • Horuk, R.1
  • 19
    • 0034792329 scopus 로고    scopus 로고
    • Use of the substituted cysteine accessibility method to study the structure and function of G protein-coupled receptors
    • Javitch JA, Shi L, and Liapakis G (2002) Use of the substituted cysteine accessibility method to study the structure and function of G protein-coupled receptors. Methods Enzymol 343:137-156.
    • (2002) Methods Enzymol , vol.343 , pp. 137-156
    • Javitch, J.A.1    Shi, L.2    Liapakis, G.3
  • 20
    • 0035497743 scopus 로고    scopus 로고
    • Is Galpha16 the optimal tool for fishing ligands of orphan G-protein-coupled receptors?
    • Kostenis E (2001) Is Galpha16 the optimal tool for fishing ligands of orphan G-protein-coupled receptors? Trends Pharmacol Sci 22:560-564.
    • (2001) Trends Pharmacol Sci , vol.22 , pp. 560-564
    • Kostenis, E.1
  • 23
    • 0034682767 scopus 로고    scopus 로고
    • Identification of the binding site for a novel class of CCR2b chemokine receptor antagonists: Binding to a common chemokine receptor motif within the helical bundle
    • Mirzadegan T, Diehl F, Ebi B, Bhakta S, Polsky I, McCarley D, Mulkins M, Weatherhead GS, Lapierre JM, Dankwardt J, et al. (2000) Identification of the binding site for a novel class of CCR2b chemokine receptor antagonists: binding to a common chemokine receptor motif within the helical bundle. J Biol Chem 275:25562-25571.
    • (2000) J Biol Chem , vol.275 , pp. 25562-25571
    • Mirzadegan, T.1    Diehl, F.2    Ebi, B.3    Bhakta, S.4    Polsky, I.5    McCarley, D.6    Mulkins, M.7    Weatherhead, G.S.8    Lapierre, J.M.9    Dankwardt, J.10
  • 26
    • 33847147674 scopus 로고    scopus 로고
    • Activation of the CXCR3 chemokine receptor through anchoring of a small molecule chelator ligand between TM-III, -IV, and -VI
    • Rosenkilde MM, Andersen MB, Nygaard R, Frimurer TM, and Schwartz TW (2007) Activation of the CXCR3 chemokine receptor through anchoring of a small molecule chelator ligand between TM-III, -IV, and -VI. Mol Pharmacol 71:930-941.
    • (2007) Mol Pharmacol , vol.71 , pp. 930-941
    • Rosenkilde, M.M.1    Andersen, M.B.2    Nygaard, R.3    Frimurer, T.M.4    Schwartz, T.W.5
  • 27
    • 33751111710 scopus 로고    scopus 로고
    • Conformational constraining of inactive and active states of a seven transmembrane receptor by metal ion site engineering in the extracellular end of transmembrane segment V
    • Rosenkilde MM, David R, Oerlecke I, ned-Jensen T, Geumann U, Beck-Sickinger AG, and Schwartz TW (2006) Conformational constraining of inactive and active states of a seven transmembrane receptor by metal ion site engineering in the extracellular end of transmembrane segment V. Mol Pharmacol 70:1892-1901.
    • (2006) Mol Pharmacol , vol.70 , pp. 1892-1901
    • Rosenkilde, M.M.1    David, R.2    Oerlecke, I.3    ned-Jensen, T.4    Geumann, U.5    Beck-Sickinger, A.G.6    Schwartz, T.W.7
  • 28
    • 0033534718 scopus 로고    scopus 로고
    • Agonists and inverse agonists for the herpesvirus 8-encoded constitutively active seven-transmembrane oncogene product, ORF-74
    • Rosenkilde MM, Kledal TN, Brauner-Osborne H, and Schwartz TW (1999) Agonists and inverse agonists for the herpesvirus 8-encoded constitutively active seven-transmembrane oncogene product, ORF-74. J Biol Chem 274:956-961.
    • (1999) J Biol Chem , vol.274 , pp. 956-961
    • Rosenkilde, M.M.1    Kledal, T.N.2    Brauner-Osborne, H.3    Schwartz, T.W.4
  • 29
    • 33746658573 scopus 로고    scopus 로고
    • GluVII:06 - a highly conserved and selective anchor point for non-peptide ligands in chemokine receptors
    • Rosenkilde MM and Schwartz TW (2006) GluVII:06 - a highly conserved and selective anchor point for non-peptide ligands in chemokine receptors. Curr Top Med Chem 6:1319-1333.
    • (2006) Curr Top Med Chem , vol.6 , pp. 1319-1333
    • Rosenkilde, M.M.1    Schwartz, T.W.2
  • 30
    • 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 Biotech 5:434-444.
    • (1994) Curr Opin Biotech , vol.5 , pp. 434-444
    • Schwartz, T.W.1
  • 32
    • 0036561677 scopus 로고    scopus 로고
    • New therapeutics that modulate chemokine networks
    • Schwarz MK and Wells TN (2002) New therapeutics that modulate chemokine networks. Nat Rev Drug Discov 1:347-358.
    • (2002) Nat Rev Drug Discov , vol.1 , pp. 347-358
    • Schwarz, M.K.1    Wells, T.N.2
  • 33
    • 0042622380 scopus 로고    scopus 로고
    • SWISS-MODEL: An automated protein homology-modeling server
    • Schwede T, Kopp J, Guex N, and Peitsch MC (2003) SWISS-MODEL: an automated protein homology-modeling server. Nucleic Acids Res 31:3381-3385.
    • (2003) Nucleic Acids Res , vol.31 , pp. 3381-3385
    • Schwede, T.1    Kopp, J.2    Guex, N.3    Peitsch, M.C.4
  • 35
    • 0037174606 scopus 로고    scopus 로고
    • Beta2 adrenergic receptor activation. Modulation of the proline kink in transmembrane 6 by a rotamer toggle switch
    • Shi L, Liapakis G, Xu R, Guarnieri F, Ballesteros JA, and Javitch JA (2002) Beta2 adrenergic receptor activation. Modulation of the proline kink in transmembrane 6 by a rotamer toggle switch. J Biol Chem 277:40989-40996.
    • (2002) J Biol Chem , vol.277 , pp. 40989-40996
    • Shi, L.1    Liapakis, G.2    Xu, R.3    Guarnieri, F.4    Ballesteros, J.A.5    Javitch, J.A.6
  • 38
    • 0037404511 scopus 로고    scopus 로고
    • Analysis of the mechanism by which the small-molecule CCR5 antagonists SCH-351125 and SCH-350581 inhibit human immunodeficiency virus type 1 entry
    • Tsamis F, Gavrilov S, Kajumo F, Seibert C, Kuhmann S, Ketas T, Trkola A, Palani A, Clader JW, Tagat JR, et al. (2003) Analysis of the mechanism by which the small-molecule CCR5 antagonists SCH-351125 and SCH-350581 inhibit human immunodeficiency virus type 1 entry. J Virol 77:5201-5208.
    • (2003) J Virol , vol.77 , pp. 5201-5208
    • Tsamis, F.1    Gavrilov, S.2    Kajumo, F.3    Seibert, C.4    Kuhmann, S.5    Ketas, T.6    Trkola, A.7    Palani, A.8    Clader, J.W.9    Tagat, J.R.10
  • 40
    • 15744391870 scopus 로고    scopus 로고
    • The CCR5 receptor-based mechanism of action of 873140, a potent allosteric noncompetitive HIV entry inhibitor
    • Watson C, Jenkinson S, Kazmierski W, and Kenakin T (2005) The CCR5 receptor-based mechanism of action of 873140, a potent allosteric noncompetitive HIV entry inhibitor. Mol Pharmacol 67:1268-1282.
    • (2005) Mol Pharmacol , vol.67 , pp. 1268-1282
    • Watson, C.1    Jenkinson, S.2    Kazmierski, W.3    Kenakin, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.