STRUCTURAL BASIS OF SH2 DOMAIN MUTATIONS IN X-LINKED AGAMMAGLOBULINEMIA

被引:36
作者
VIHINEN, M
NILSSON, L
SMITH, CIE
机构
[1] UNIV TURKU, DEPT BIOCHEM, SF-20500 TURKU, FINLAND
[2] KAROLINSKA INST, NOVUM, CTR BIOTECHNOL, S-14157 HUDDINGE, SWEDEN
[3] KAROLINSKA INST, HUDDINGE HOSP, DEPT CLIN IMMUNOL, S-14186 HUDDINGE, SWEDEN
关键词
D O I
10.1006/bbrc.1994.2802
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
The three-dimensional structure of Bruton's agammaloglobulinemia tyrosine kinase (Btk) SH2 domain was modeled based on v-Src. Btk SH2 is presumably very related to the other SH2 structures consisting of two beta-sheets surrounded by two alpha-helices, with a well conserved hydrophobic core and phoshotyrosyl peptide binding site. The model was used to predict the recognition sequence of the target protein, which probably is YEXI/L. Mutations in the Btk sequence can cause the human disease X-linked agammaglobulinemia and reasons for the disease in Btk SH2 mutations were inferred from the model. (C) 1994 Academic Press, Inc.
引用
收藏
页码:1270 / 1277
页数:8
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