2BVE
Structure of the N-terminal of Sialoadhesin in complex with 2-Phenyl- Prop5Ac
2BVE の概要
エントリーDOI | 10.2210/pdb2bve/pdb |
関連するPDBエントリー | 1OD7 1OD9 1ODA 1QFO 1QFP 1URL |
分子名称 | SIALOADHESIN, benzyl 3,5-dideoxy-5-(propanoylamino)-D-glycero-alpha-D-galacto-non-2-ulopyranosidonic acid (3 entities in total) |
機能のキーワード | immune system, immunoglobulin, lectin, superfamily, carbohydrate binding, siglec, inhibitor design, cell adhesion |
由来する生物種 | MUS MUSCULUS (MOUSE) |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 27465.05 |
構造登録者 | Zaccai, N.R.,May, A.P.,Robinson, R.C.,Burtnick, L.D.,Crocker, P.,Brossmer, R.,Kelm, S.,Jones, E.Y. (登録日: 2005-06-27, 公開日: 2006-07-19, 最終更新日: 2024-11-06) |
主引用文献 | Zaccai, N.R.,May, A.P.,Robinson, R.C.,Burtnick, L.D.,Crocker, P.,Brossmer, R.,Kelm, S.,Jones, E.Y. Crystallographic and in Silico Analysis of the Sialoside-Binding Characteristics of the Siglec Sialoadhesin. J.Mol.Biol., 365:1469-, 2007 Cited by PubMed Abstract: The Siglec family of receptors mediates cell-surface interactions through recognition of sialylated glycoconjugates. Previously reported structures of the N-terminal domain of the Siglec sialoadhesin (SnD1) in complex with various sialic acid analogs revealed the structural template for sialic acid binding. To characterize further the carbohydrate-binding properties, we have determined the crystal structures of SnD1 in the absence of ligand, and in complex with 2-benzyl-Neu5NPro and 2-benzyl-Neu5NAc. These structures reveal that SnD1 undergoes very few structural changes on ligand binding and detail how two novel classes of sialic acid analogs bind, one of which unexpectedly can induce Siglec dimerization. In conjunction with in silico analysis, this set of structures informs us about the design of putative ligands with enhanced binding affinities and specificities to different Siglecs, and provides data with which to test the effectiveness of different computational drug design protocols. PubMed: 17137591DOI: 10.1016/J.JMB.2006.10.084 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.2 Å) |
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