1nr2 Citations

Structures of thymus and activation-regulated chemokine (TARC).

Acta Crystallogr D Biol Crystallogr 59 1165-73 (2003)
Cited: 13 times
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Abstract

Thymus and activation-regulated chemokine (TARC) is a CC chemokine that is mainly expressed in the thymus. TARC interacts primarily with the CCR4 receptor and to a lesser extent with the CCR8 receptor. The structures of TARC have been solved by molecular replacement in two space groups, triclinic (P1) and tetragonal (P4(1)), and refined to resolutions of 1.72 and 2.1 A, respectively, with R factors of 19.8% (R(free) = 24.1%) and 19.8% (R(free) = 27.7%), respectively. The search model originated from the crystal structure of another chemokine, RANTES, and proved to be only modestly similar to the refined structure of TARC. Whereas the tetragonal structure was easily solved using the program AMoRe, solution of the triclinic structure proved to be quite challenging and was obtained by combining the results from four different molecular-replacement programs (AMoRe, CNS, BEAST and EPMR), with subsequent extension of the gathered information. The tertiary structure of TARC is similar to that of other CC chemokines, with a three-stranded antiparallel beta-sheet flanked by a C-terminal helix. Both quaternary structures consist of dimers, which in the triclinic crystals pack further into tetramers. The TARC dimers are similar to those observed previously in the crystal structures of both MCP-1 and RANTES.

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  1. Computational protein design: validation and possible relevance as a tool for homology searching and fold recognition. Schmidt Am Busch M, Sedano A, Simonson T. PLoS One 5 e10410 (2010)
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  1. Chemokine oligomerization in cell signaling and migration. Wang X, Sharp JS, Handel TM, Prestegard JH. Prog Mol Biol Transl Sci 117 531-578 (2013)

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  1. X-ray structure of Na-ASP-2, a pathogenesis-related-1 protein from the nematode parasite, Necator americanus, and a vaccine antigen for human hookworm infection. Asojo OA, Goud G, Dhar K, Loukas A, Zhan B, Deumic V, Liu S, Borgstahl GE, Hotez PJ. J Mol Biol 346 801-814 (2005)
  2. RNA Aptamers Recognizing Murine CCL17 Inhibit T Cell Chemotaxis and Reduce Contact Hypersensitivity In Vivo. Fülle L, Steiner N, Funke M, Gondorf F, Pfeiffer F, Siegl J, Opitz FV, Haßel SK, Erazo AB, Schanz O, Stunden HJ, Blank M, Gröber C, Händler K, Beyer M, Weighardt H, Latz E, Schultze JL, Mayer G, Förster I. Mol Ther 26 95-104 (2018)
  3. A strategy to discover decoy chemokine ligands with an anti-inflammatory activity. Abboud D, Daubeuf F, Do QT, Utard V, Villa P, Haiech J, Bonnet D, Hibert M, Bernard P, Galzi JL, Frossard N. Sci Rep 5 14746 (2015)
  4. Crystal structure of viral macrophage inflammatory protein I encoded by Kaposi's sarcoma-associated herpesvirus at 1.7A. Luz JG, Yu M, Su Y, Wu Z, Zhou Z, Sun R, Wilson IA. J Mol Biol 352 1019-1028 (2005)
  5. The role of alcohol on platelets, thymus and cognitive performance among HIV-infected subjects: are they related? Míguez-Burbano MJ, Nair M, Lewis JE, Fishman J. Platelets 20 260-267 (2009)
  6. Internalization of CCR4 and inhibition of chemotaxis by K777, a potent and selective CCR4 antagonist. Sato T, Iwase M, Miyama M, Komai M, Ohshima E, Asai A, Yano H, Miki I. Pharmacology 91 305-313 (2013)
  7. Surrogate antibodies that specifically bind and neutralize CCL17 but not CCL22. Santulli-Marotto S, Fisher J, Petley T, Boakye K, Panavas T, Luongo J, Kavalkovich K, Rycyzyn M, Wu B, Gutshall L, Coelho A, Hogaboam CM, Ryan M. Monoclon Antib Immunodiagn Immunother 32 162-171 (2013)
  8. N-terminal Backbone Pairing Shifts in CCL5-12AAA14 Dimer Interface: Structural Significance of the FAY Sequence. Li JY, Chen YC, Lee YZ, Huang CH, Sue SC. Int J Mol Sci 21 E1689 (2020)


Related citations provided by authors (1)

  1. Crystallization and preliminary X-ray studies of thymus and activation-regulated chemokine. Asojo OA, Hoover D, Boulegue C, Cater S, Lu W, Lubkowski J Acta Crystallogr. D Biol. Crystallogr. 59 163-165 (2003)