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1O7Z

Crystal structure of IP-10 T-form

1O7Z の概要
エントリーDOI10.2210/pdb1o7z/pdb
関連するPDBエントリー1LV9 1O7Y 1O80
分子名称SMALL INDUCIBLE CYTOKINE B10 (2 entities in total)
機能のキーワードchemokine, interferon induction, chemotaxis, inflammatory response
由来する生物種HOMO SAPIENS (HUMAN)
細胞内の位置Secreted: P02778
タンパク質・核酸の鎖数2
化学式量合計17274.69
構造登録者
Swaminathan, G.J.,Holloway, D.E.,Papageorgiou, A.C.,Acharya, K.R. (登録日: 2002-11-20, 公開日: 2003-05-08, 最終更新日: 2024-11-13)
主引用文献Swaminathan, G.J.,Holloway, D.E.,Colvin, R.A.,Campanella, G.K.,Papageorgiou, A.C.,Luster, A.D.,Acharya, K.R.
Crystal Structures of Oligomeric Forms of the Ip-10/Cxcl10 Chemokine
Structure, 11:521-, 2003
Cited by
PubMed Abstract: We have determined the structure of wild-type IP-10 from three crystal forms. The crystals provide eight separate models of the IP-10 chain, all differing substantially from a monomeric IP-10 variant examined previously by NMR spectroscopy. In each crystal form, IP-10 chains form conventional beta sheet dimers, which, in turn, form a distinct tetrameric assembly. The M form tetramer is reminiscent of platelet factor 4, whereas the T and H forms feature a novel twelve-stranded beta sheet. Analytical ultracentrifugation indicates that, in free solution, IP-10 exists in a monomer-dimer equilibrium with a dissociation constant of 9 microM. We propose that the tetrameric structures may represent species promoted by the binding of glycosaminoglycans. The binding sites for several IP-10-neutralizing mAbs have also been mapped.
PubMed: 12737818
DOI: 10.1016/S0969-2126(03)00070-4
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.92 Å)
構造検証レポート
Validation report summary of 1o7z
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-12-24に公開中

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