Solution structure of the link module: A hyaluronan-binding domain involved in extracellular matrix stability and cell migration

被引:254
作者
Kohda, D
Morton, CJ
Parkar, AA
Hatanaka, H
Inagaki, FM
Campbell, ID
Day, AJ
机构
[1] UNIV OXFORD,DEPT BIOCHEM,OXFORD OX1 3QU,ENGLAND
[2] UNIV OXFORD,OXFORD CTR MOL SCI,OXFORD OX1 3QU,ENGLAND
[3] TOKYO METROPOLITAN INST MED SCI,BUNKYO KU,TOKYO 113,JAPAN
基金
英国惠康基金;
关键词
D O I
10.1016/S0092-8674(00)80151-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Link modules are hyaluronan-binding domains found in proteins involved in the assembly of extracellular matrix, cell adhesion, and migration. The solution structure of the Link module from human TSG-6 was determined and found to consist of two alpha helices and two antiparallel beta sheets arranged around a large hydrophobic core. This defines the consensus fold for the Link module superfamily, which includes CD44, cartilage link protein, and aggrecan. The TSG-6 Link module was shown to interact with hyaluronan, and a putative binding surface was identified on the structure. A structural database search revealed close similarity between the Link module and the C-type lectin domain, with the predicted hyaluronan-binding site at an analogous position to the carbohydrate-binding pocket in E-selectin.
引用
收藏
页码:767 / 775
页数:9
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