Human members of the eukaryotic protein kinase family.

@article{citeulike:2906078, abstract = {BACKGROUND: Eukaryotic protein kinases (EPKs) constitute one of the largest recognized protein families represented in the human genome. EPKs, which are similar to each other in sequence, structure and biochemical properties, are important players in virtually every signaling pathway involved in normal development and disease. Near completion of projects to sequence the human genome and transcriptome provide an opportunity to identify and perform sequence analysis on a nearly complete set of human EPKs. RESULTS: Publicly available genetic sequence data were searched for human sequences that potentially represent EPK family members. After removal of duplicates, splice variants and pseudogenes, this search yielded 510 sequences with recognizable similarity to the EPK family. Protein sequences of putative EPK catalytic domains identified in the search were aligned, and a phonogram was constructed based on the alignment. Representative sequence records in GenBank were identified, and derived information about gene mapping and nomenclature was summarized. CONCLUSIONS: This work represents a nearly comprehensive census and early bioinformatics overview of the EPKs encoded in the human genome. Evaluation of the sequence relationships between these proteins contributes contextual information that enhances understanding of individual family members. This curation of human EPK sequences provides tools and a framework for the further characterization of this important class of enzymes.}, address = {Discovery Technology, Schering-Plough Research Institute, Kenilworth, NJ 07033, USA. mitchell.kostich@spcorp.com}, author = {Kostich, M. and English, J. and Madison, V. and Gheyas, F. and Wang, L. and Qiu, P. and Greene, J. and Laz, T. M. }, citeulike-article-id = {2906078}, issn = {1465-6914}, journal = {Genome biology}, keywords = {kinase, kinome}, month = {August}, number = {9}, posted-at = {2008-06-18 20:39:48}, priority = {2}, title = {Human members of the eukaryotic protein kinase family.}, url = {http://view.ncbi.nlm.nih.gov/pubmed/12225582}, volume = {3}, year = {2002} }

TY - JOUR ID - citeulike:2906078 L3 - citeulike-article-id:2906078 TI - Human members of the eukaryotic protein kinase family. JF - Genome biology VL - 3 IS - 9 AD - Discovery Technology, Schering-Plough Research Institute, Kenilworth, NJ 07033, USA. mitchell.kostich@spcorp.com SN - 1465-6914 N2 - BACKGROUND: Eukaryotic protein kinases (EPKs) constitute one of the largest recognized protein families represented in the human genome. EPKs, which are similar to each other in sequence, structure and biochemical properties, are important players in virtually every signaling pathway involved in normal development and disease. Near completion of projects to sequence the human genome and transcriptome provide an opportunity to identify and perform sequence analysis on a nearly complete set of human EPKs. RESULTS: Publicly available genetic sequence data were searched for human sequences that potentially represent EPK family members. After removal of duplicates, splice variants and pseudogenes, this search yielded 510 sequences with recognizable similarity to the EPK family. Protein sequences of putative EPK catalytic domains identified in the search were aligned, and a phonogram was constructed based on the alignment. Representative sequence records in GenBank were identified, and derived information about gene mapping and nomenclature was summarized. CONCLUSIONS: This work represents a nearly comprehensive census and early bioinformatics overview of the EPKs encoded in the human genome. Evaluation of the sequence relationships between these proteins contributes contextual information that enhances understanding of individual family members. This curation of human EPK sequences provides tools and a framework for the further characterization of this important class of enzymes. KW - kinase KW - kinome AU - Kostich, M AU - English, J AU - Madison, V AU - Gheyas, F AU - Wang, L AU - Qiu, P AU - Greene, J AU - Laz, TM PY - 2002/08/22/ UR - http://view.ncbi.nlm.nih.gov/pubmed/12225582 ER -