| Literature DB >> 11169590 |
J Bandorowicz-Pikula1, R Buchet, S Pikula.
Abstract
Annexins are ubiquitous multifunctional Ca2+ and phospholipid-binding proteins whose mechanism of function remains largely unknown. The accumulated in vitro experimental evidence indicates that ATP and GTP are functional ligands for nucleotide-sensitive annexin isoforms. Such nucleotide binding could modulate Ca2+ homeostasis, vesicular transport and/or signal transduction pathways and link them to cellular energy metabolism. Alternatively, since annexins are able to interact with other nucleotide-utilizing proteins, such as various kinases, GTPases and structural proteins, these proteins could influence the guanine nucleotide exchange metabolism and/or control the activity of various G proteins. The nucleotide-binding properties of annexins may affect the development or maintenance of some pathologies and diseases in which changes in physiological concentrations of purine nucleotides or disruption of Ca2+ homeostasis are crucial targets.Entities:
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Year: 2001 PMID: 11169590 DOI: 10.1002/1521-1878(200102)23:2<170::AID-BIES1024>3.0.CO;2-#
Source DB: PubMed Journal: Bioessays ISSN: 0265-9247 Impact factor: 4.345