Nucleic Acids Research, Vol 27, Issue 1 362-364, Copyright © 1999 by Oxford University Press
KA Stenberg, PT Riikonen and M Vihinen
KinMutBase (http://www.uta.fi/laitokset/imt/KinMut Base.html) is a registry
of mutations in human protein kinases related to disorders. Kinases are
essential cellular signalling molecules, in which mutations can lead into
diseases including, e.g., immunodeficiencies, cancers and endocrine
disorders. The first release of KinMutBase contains information for nine
protein tyrosine kinases. There are altogether 170 entries representing 273
families and 403 patients. Mutations appear both in conserved hallmark
residues of the kinases as well as in non- homologous sites. The KinMutBase
WWW pages provide plenty of information, namely mutation statistics and
display, clickable sequences with mutations, restriction enzyme patterns
and online submission.
ARTICLES
KinMutBase, a database of human disease-causing protein kinase mutations
Department of Biosciences, Division of Biochemistry, PO Box 56, FIN- 00014, University of Helsinki, Helsinki, Finland.
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