Rn. Haire et al., TXK, A NOVEL HUMAN TYROSINE KINASE EXPRESSED IN T-CELLS SHARES SEQUENCE IDENTITY WITH TEC FAMILY KINASES AND MAPS TO 4P12, Human molecular genetics, 3(6), 1994, pp. 897-901
A gene for a novel, putative cytoplasmic tyrosine kinase, TXK has been
isolated from a human peripheral blood cDNA library. The complete nuc
leotide sequence of the cDNA indicates that it is related mast closely
to EMT, a tyrosine kinase of T cells and to the B-cell tyrosine kinas
e Btk, which is mutated in X-linked agammaglobulinemia (XLA) in humans
and X-linked immunodeficiency disease (XID) in mouse. TXK, like BTK,
is a member of the Tec sub-family of Src-type (non-receptor) tyrosine
kinases. Like similar Tec subfamily members, and unlike the other Src
kinases, TXK lacks both the N-terminal myristylation signal and the C-
terminal regulatory tyrosine. TXK expression is detected primarily in
T cells and some myeloid cell lines but not in a number of other cell
types. TXK shares 60% amino acid homology with EMT and 57% with BTK ov
er the SH3, SH2 (Src-homology) and catalytic domains but unlike BTK, E
MT and tee, it lacks Gap 1 homology and steroid hormone receptor homol
ogy in the N-terminal region. Genomic clones containing TXK have been
isolated and hybridize to chromosome position 4p12.