3GXY

Crystal structure of cyanovirin-n complexed to a synthetic hexamannoside

「1M5J」から置き換えられました

3GXY の概要

• エントリーDOI: 10.2210/pdb3gxy/pdb
• 関連するPDBエントリー: 1M5J 1M5M 3GXZ
• 分子名称: Cyanovirin-N, alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-pentyl alpha-D-mannopyranoside, 2-[N-CYCLOHEXYLAMINO]ETHANE SULFONIC ACID, ... (5 entities in total)
• 機能のキーワード: cyanovirin-n, hiv-inactivating, domain-swapping, gp120, man-9, oligosaccharide, antiviral protein, disulfide bond, protein synthesis inhibitor
• 由来する生物種: Nostoc ellipsosporum
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 23424.92

構造登録者

Botos, I.,O'Keefe, B.R.,Shenoy, S.R.,Seeberger, P.H.,Boyd, M.R.,Wlodawer, A. (登録日: 2009-04-03, 公開日: 2009-05-05, 最終更新日: 2023-09-06)

主引用文献

Botos, I.,O'Keefe, B.R.,Shenoy, S.R.,Cartner, L.K.,Ratner, D.M.,Seeberger, P.H.,Boyd, M.R.,Wlodawer, A.
Structures of the complexes of a potent anti-HIV protein cyanovirin-n and high mannose oligosaccharides
J.Biol.Chem., 277:34336-34342, 2002

PubMed Abstract: The development of anti-human immunodeficiency virus (HIV) microbicides for either topical or ex vivo use is of considerable interest, mainly due to the difficulties in creating a vaccine that would be active against multiple clades of HIV. Cyanovirin-N (CV-N), an 11-kDa protein from the cyanobacterium (blue-green algae) Nostoc ellipsosporum with potent virucidal activity, was identified in the search for such antiviral agents. The binding of CV-N to the heavily glycosylated HIV envelope protein gp120 is carbohydrate-dependent. Since previous CV-N-dimannose structures could not fully explain CV-N-oligomannose binding, we determined the crystal structures of recombinant CV-N complexed to Man-9 and a synthetic hexamannoside, at 2.5- and 2.4-A resolution, respectively. CV-N is a three-dimensional domain-swapped dimer in the crystal structures with two primary sites near the hinge region and two secondary sites on the opposite ends of the dimer. The binding interface is constituted of three stacked alpha1-->2-linked mannose rings for Man-9 and two stacked mannose rings for hexamannoside with the rest of the saccharide molecules pointing to the solution. These structures show unequivocally the binding geometry of high mannose sugars to CV-N, permitting a better understanding of carbohydrate binding to this potential new lead for the design of drugs against AIDS.

PubMed: 12110688
DOI: 10.1074/jbc.M205909200

実験手法

X-RAY DIFFRACTION (2.4 Å)