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.