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Cx23, a connexin with only four extracellular-loop cysteines, forms functional gap junction channels and hemichannels
- Source :
- FEBS letters. 582(2)
- Publication Year :
- 2007
-
Abstract
- Gap junction channels may be comprised of either connexin or pannexin proteins (innexins and pannexins). Membrane topologies of both families are similar, but sequence similarity is lacking. Recently, connexin-like sequences have been identified in mammalian and zebrafish genomes that have only four conserved cysteines in the extracellular domains (Cx23), a feature of the pannexins. Phylogenetic analyses of the non-canonical “C4” connexins reveal that these sequences are indeed connexins. Functional assays reveal that the Cx23 gap junctions are capable of sharing neurobiotin, and further, that Cx23 connexins form hemichannels in vitro.
- Subjects :
- Gap junction
Molecular Sequence Data
Biophysics
Connexin
Biology
Pannexin
Biochemistry
Connexins
Article
Structural Biology
Lens, Crystalline
Genetics
Extracellular
otorhinolaryngologic diseases
Animals
Humans
Base sequence
Amino Acid Sequence
Cysteine
Molecular Biology
Peptide sequence
Zebrafish
Lens crystalline
In Situ Hybridization
DNA Primers
Base Sequence
Sequence Homology, Amino Acid
Gap Junctions
Cell Biology
biology.organism_classification
Cx23
Cell biology
sense organs
HeLa Cells
Subjects
Details
- ISSN :
- 00145793
- Volume :
- 582
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- FEBS letters
- Accession number :
- edsair.doi.dedup.....4b2ac0dcb4c837da7a853907176e6f70