1SHU

Crystal Structure of the von Willebrand factor A domain of human capillary morphogenesis protein 2: an anthrax toxin receptor

1SHU の概要

• エントリーDOI: 10.2210/pdb1shu/pdb
• 関連するPDBエントリー: 1SHT
• 分子名称: Anthrax toxin receptor 2, MAGNESIUM ION (3 entities in total)
• 機能のキーワード: alpha/beta rossmann fold, membrane protein
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Isoform 1: Cell membrane; Single-pass type I membrane protein. Isoform 2: Endoplasmic reticulum membrane; Single-pass type I membrane protein. Isoform 3: Secreted: P58335
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 19922.15

構造登録者

Lacy, D.B.,Wigelsworth, D.J.,Scobie, H.M.,Young, J.A.T.,Collier, R.J. (登録日: 2004-02-26, 公開日: 2004-04-13, 最終更新日: 2024-11-13)

主引用文献

Lacy, D.B.,Wigelsworth, D.J.,Scobie, H.M.,Young, J.A.T.,Collier, R.J.
Crystal Structure of the von Willebrand factor A domain of human capillary morphogenesis protein 2: an anthrax toxin receptor
Proc.Natl.Acad.Sci.USA, 101:6367-6372, 2004

PubMed Abstract: Anthrax toxin is released from Bacillus anthracis as three monomeric proteins, which assemble into toxic complexes at the surface of receptor-bearing host cells. One of the proteins, protective antigen (PA), binds to receptors and orchestrates the delivery of the other two (the lethal and edema factors) into the cytosol. PA has been shown to bind to two cellular receptors: anthrax toxin receptor/tumor endothelial marker 8 and capillary morphogenesis protein 2 (CMG2). Both are type 1 membrane proteins that include an approximately 200-aa extracellular von Willebrand factor A (VWA) domain with a metal ion-dependent adhesion site (MIDAS) motif. The anthrax toxin receptor/tumor endothelial marker 8 and CMG2 VWA domains share approximately 60% amino acid identity and bind PA directly in a metal-dependent manner. Here, we report the crystal structure of the CMG2 VWA domain, with and without its intramolecular disulfide bond, to 1.5 and 1.8 A, respectively. Both structures contain a carboxylate ligand-mimetic bound at the MIDAS and appear as open conformations when compared with the VWA domains from alpha-integrins. The CMG2 structures provide a template to begin probing the high-affinity CMG2-PA interaction (200 pM) and may facilitate understanding of toxin assembly/internalization and the development of new anthrax treatments. The structural data also allow molecular interpretation of known CMG2 VWA domain mutations linked to the genetic disorders, juvenile hyaline fibromatosis, and infantile systemic hyalinosis.

PubMed: 15079089
DOI: 10.1073/pnas.0401506101

実験手法

X-RAY DIFFRACTION (1.5 Å)