1O7Y
Crystal structure of IP-10 M-form
1O7Y の概要
| エントリーDOI | 10.2210/pdb1o7y/pdb |
| 関連するPDBエントリー | 1LV9 1O7Z 1O80 |
| 分子名称 | SMALL INDUCIBLE CYTOKINE B10, SULFATE ION (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) |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 34741.51 |
| 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: 2024-10-23) |
| 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: 12737818DOI: 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 (3 Å) |
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