The Kabat Database was initially started in 1970 to determine the combining
site of antibodies based on the available amino acid sequences. The precis
e delineation of complementarity determining regions (CDR) of both light an
d heavy chains provides the first example of how property aligned sequences
can be used to derive structural and functional information of biological
macromolecules, This knowledge has subsequently been applied to the constru
ction of artificial antibodies with prescribed specificities, and to many o
ther studies. The Kabat database now includes nucleotide sequences, sequenc
es of T cell receptors for antigens (TCR), major histocompatibility complex
(MHC) class I and II molecules, and other proteins of immunological intere
st. While new sequences are continually added into this database, we have u
ndertaken the task of developing more analytical methods to study the infor
mation content of this collection of aligned sequences. New examples of ana
lysis will be illustrated on a yearly basis. The Kabat Database and its app
lications are freely available at http://immuno.bme.nwu.edu.