Bruton tyrosine kinase (Btk) in X-linked agammaglobulinemia (XLA)

Citation
M. Vihinen et al., Bruton tyrosine kinase (Btk) in X-linked agammaglobulinemia (XLA), FRONT BIOSC, 5, 2000, pp. D917-D927
Citations number
139
Categorie Soggetti
Biochemistry & Biophysics
Journal title
FRONTIERS IN BIOSCIENCE
ISSN journal
10939946 → ACNP
Volume
5
Year of publication
2000
Pages
D917 - D927
Database
ISI
SICI code
1093-9946(200012)5:<D917:BTK(IX>2.0.ZU;2-1
Abstract
X-linked agammaglobulinemia (XLA) is a heritable immunodeficiency disorder that is caused by a differentiation block leading to almost complete absenc e of B lymphocytes and plasma cells. The affected protein is a cytoplasmic protein tyrosine kinase, Bruton's agammaglobulinemia tyrosine kinase (Btk). Btk along with Tec, Itk, Bmx and Txk belong to a distinct family of protei n kinases. These proteins contain five regions; PH, TH, SH3, SH2 and kinase domains. Mutations causing XLA may affect any of these domains. About 380 unique mutations have been identified and are collected in a mutation datab ase, BTKbase. Here, we describe the structure, function, and interactions o f the affected signaling molecules in atomic detail.