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G. Manning,1*D. B. Whyte,1R. Martinez,1T. Hunter,2S. Sudarsanam13
We have catalogued the protein kinase complement of the
human genome (the "kinome") using public and proprietary genomic,complementary DNA, and expressed sequence tag (EST) sequences.This
provides a starting point for comprehensive analysis of proteinphosphorylation in normal and disease states, as well as a
detailedview of the current state of human genome analysis through a
focuson one large gene family. We identify 518 putative protein kinasegenes, of which 71 have not previously been reported or describedas
kinases, and we extend or correct the protein sequences of56 more
kinases. New genes include members of well-studied familiesas well as
previously unidentified families, some of which areconserved in model
organisms. Classification and comparison withmodel organism kinomes
identified orthologous groups and highlightedexpansions specific to
human and other lineages. We also identified106 protein kinase
pseudogenes. Chromosomal mapping revealed severalsmall clusters of
kinase genes and revealed that 244 kinases mapto disease loci or
cancer amplicons.
1 SUGEN Inc., 230 East Grand Avenue, South San
Francisco, CA 94080, USA.
2 Salk Institute, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
3 Genomics
and Biotechnology, Pharmacia Corporation, 230 East Grand Avenue, South
San Francisco, CA 94080, USA.
*
To whom correspondence should be addressed. E-mail:
gerard-manning{at}sugen.com
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