Spectrin: Difference between revisions

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[[Spectrin]] forms scaffolding in plasma membranes and cytoskeletal structure.  It interacts with actin at either end of its tetramer<ref>PMID:17060500</ref>.  The SPT dimer is formed by association of α1 and β1 monomers.  In invertebrates there are SPT α, β and βH.  In vertebrates there are SPT α1 (SPTA1), α2 (SPTA2) and β1 (SPTB1) to β5.  SPT contains an SRC Homology 3 domain (SH3), a Pleckstrin Homology (PH) domain and a Calponin Homology (CH) domain.  
[[Spectrin]] forms scaffolding in plasma membranes and cytoskeletal structure.  It interacts with actin at either end of its tetramer<ref>PMID:17060500</ref>.  The SPT dimer is formed by association of α1 and β1 monomers.  In invertebrates there are SPT α, β and βH.  In vertebrates there are SPT α1 (SPTA1), α2 (SPTA2) and β1 (SPTB1) to β5.  SPT contains an SRC Homology 3 domain (SH3), a Pleckstrin Homology (PH) domain and a Calponin Homology (CH) domain.  
*'''Spectrin α2''' is expressed highly in heart muscle cells<ref>PMID:15360127</ref>.  
*'''Spectrin α2''' is expressed highly in heart muscle cells<ref>PMID:15360127</ref>.  
*'''Spectrin β2''' is associated with GABA receptor at dendritic synapses<ref>PMID:36604600</ref>.
*'''Spectrin β4''' is associated with GABA receptor at axon initial segment synapses.


== Disease ==
== Disease ==

Revision as of 10:31, 13 August 2024

Human spectrinα (grey) and β1 chain (green) 3lbx

Drag the structure with the mouse to rotate

References

Proteopedia Page Contributors and Editors (what is this?)

Alexander Berchansky, Michal Harel