Spectrin: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
Michal Harel (talk | contribs)
No edit summary
Michal Harel (talk | contribs)
No edit summary
Line 36: Line 36:
**[[1e6g]], [[1e6h]], [[1hd3]], [[1qkx]], [[1pwt]], [[1bk2]], [[1shg]], [[1h8k]], [[3ngp]], [[3m0p]], [[3m0q]], [[3m0r]], [[3m0s]], [[3m0t]], [[3m0u]] - cSPT a chain SH3 domain (mutant)<br />
**[[1e6g]], [[1e6h]], [[1hd3]], [[1qkx]], [[1pwt]], [[1bk2]], [[1shg]], [[1h8k]], [[3ngp]], [[3m0p]], [[3m0q]], [[3m0r]], [[3m0s]], [[3m0t]], [[3m0u]] - cSPT a chain SH3 domain (mutant)<br />
**[[1uue]], [[1e7o]], [[1g2b]], [[1aey]], [[1tuc]], [[1tud]] - cSPT a chain SH3 domain (mutant) – NMR<br />
**[[1uue]], [[1e7o]], [[1g2b]], [[1aey]], [[1tuc]], [[1tud]] - cSPT a chain SH3 domain (mutant) – NMR<br />
**[[2lj3]] - cSPT a chain SH3 domain – NMR<br />
**[[2lj3]], [[6scw]] - cSPT a chain SH3 domain – NMR<br />
**[[1u4q]] – cSPT a chain repeats 15-17 1662-1982<br />
**[[1u4q]] – cSPT a chain repeats 15-17 1662-1982<br />
**[[1u5p]] - cSPT a chain repeats 15-16 1662-1876<br />
**[[1u5p]] - cSPT a chain repeats 15-16 1662-1876<br />
**[[1cun]] - cSPT a chain repeats 16-17 (mutant) 1771-1982<br />
**[[1cun]] - cSPT a chain repeats 16-17 (mutant) 1771-1982<br />
**[[1aj3]] - cSPT a chain repeat 16 1772-1869 - NMR<br />
**[[1aj3]] - cSPT a chain repeat 16 1772-1869 - NMR<br />
**[[6ro9]] – SPT SH3 domain – sunfish<br />


* Spectrin β1
* Spectrin β1
Line 57: Line 58:
**[[1wjm]] – hSPT β3 chain PH domain 2199-2328 – NMR<br />
**[[1wjm]] – hSPT β3 chain PH domain 2199-2328 – NMR<br />
**[[6anu]] - hSPT β3 chain actin binding domain 1-284 + actin - Cryo EM<br />
**[[6anu]] - hSPT β3 chain actin binding domain 1-284 + actin - Cryo EM<br />
* Spectrin β4
**[[6m3r]] – mSPT b chain 1616-1937 + Ankyrin-3<br />
**[[6m3q]] – mSPT b chain + Ankyrin-2<br />


* Spectrin β
* Spectrin β
Line 62: Line 68:
**[[1bkr]], [[1aa2]] – hSPT β chain 2nd CH domain 178-291<br />
**[[1bkr]], [[1aa2]] – hSPT β chain 2nd CH domain 178-291<br />
**[[1dro]], [[1mph]] - mSPT β chain PH domain 2199-2304 – NMR – mouse<br />
**[[1dro]], [[1mph]] - mSPT β chain PH domain 2199-2304 – NMR – mouse<br />
**[[1btn]] – mSPT β chain PH domain +inositol phosphate<br />
**[[1btn]] – mSPT β chain PH domain + inositol phosphate<br />
**[[6m3p]] – mSPT β 2 chain 1591-1910 + Ankyrin-3<br />
**[[2spc]] – SPT fragment 1391-1497 - ''Drosophila melanogaster''
**[[2spc]] – SPT fragment 1391-1497 - ''Drosophila melanogaster''



Revision as of 11:56, 11 November 2020

Function

Spectrin forms scaffolding in plasma membranes and cytoskeletal structure. It interacts with actin at either end of its tetramer[1]. 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.

Disease

Mutations in SPT α are found in patients with hereditary elliptocytosis[2]. SPT β deficiency is found in hereditary spherocytosis[3].

Human spectrin α (grey) and β1 chain (green) 3lbx

Drag the structure with the mouse to rotate

3D Structures of Spectrin3D Structures of Spectrin

Updated on 11-November-2020

ReferencesReferences

  1. Das A, Base C, Dhulipala S, Dubreuil RR. Spectrin functions upstream of ankyrin in a spectrin cytoskeleton assembly pathway. J Cell Biol. 2006 Oct 23;175(2):325-35. PMID:17060500 doi:http://dx.doi.org/10.1083/jcb.200602095
  2. Coetzer T, Palek J, Lawler J, Liu SC, Jarolim P, Lahav M, Prchal JT, Wang W, Alter BP, Schewitz G, et al.. Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis. Blood. 1990 Jun 1;75(11):2235-44. PMID:2346784
  3. Dhermy D, Galand C, Bournier O, Cynober T, Mechinaud F, Tchemia G, Garbarz M. Hereditary spherocytosis with spectrin deficiency related to null mutations of the beta-spectrin gene. Blood Cells Mol Dis. 1998 Jun;24(2):251-61. PMID:9714702 doi:http://dx.doi.org/10.1006/bcmd.1998.0190

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

Alexander Berchansky, Michal Harel