Plectin: Difference between revisions
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<Structure load='1sh6' size='400' caption='Mouse plectin actin-binding domain [[1sh6]]' scene= '> | <Structure load='1sh6' size='400' caption='Mouse plectin actin-binding domain [[1sh6]]' scene= '> | ||
== Function == | == Function == | ||
'''Plectin''', a universal and functionally versatile cytolinker protein, can be divided in three main sections; a central coiled-coil rod domain (residues 1492-1530), N and C-terminal globular region and exhibits a dumbbell like structure <ref>PMID:3430617</ref>. C-terminal region is composed of 6 homologous repeating domains (repeat#6 contains residues 4403-4606), and this region has a role in binding to intermediate filaments such as vimentin and cytokeratin<ref>PMID:24810881</ref>, <ref>PMID:24940650</ref>. N-terminal globular region contains actin binding domain (ABD) (residues 175-400) comprising of two calponin homology (CH) domains, plakin domain (residues | '''Plectin''', a universal and functionally versatile cytolinker protein, can be divided in three main sections; a central coiled-coil rod domain (residues 1492-1530), N and C-terminal globular region and exhibits a dumbbell like structure <ref>PMID:3430617</ref>. C-terminal region is composed of 6 homologous repeating domains (repeat#6 contains residues 4403-4606), and this region has a role in binding to intermediate filaments such as vimentin and cytokeratin<ref>PMID:24810881</ref>, <ref>PMID:24940650</ref>. N-terminal globular region contains actin binding domain (ABD) (residues 175-400) comprising of two calponin homology (CH) domains, plakin domain (residues 300-1372) and N-terminal arm, which varies among isoforms. | ||
For more details see [[Group:MUZIC:Plectin]]. | For more details see [[Group:MUZIC:Plectin]]. | ||
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[[1mb8]], [[4q59]] – hPCN actin-binding domain – human<br /> | [[1mb8]], [[4q59]] – hPCN actin-binding domain – human<br /> | ||
[[1sh5]], [[1sh6]] - PCN actin-binding domain – mouse<br /> | [[1sh5]], [[1sh6]] - PCN actin-binding domain – mouse<br /> | ||
[[3pe0]] - hPCN plakin domain residues 747-918<br /> | |||
[[2odu]], [[2odv]] – hPCN plakin domain (mutant)<br /> | [[2odu]], [[2odv]] – hPCN plakin domain residues 300-530 (mutant)<br /> | ||
[[3pdy]] – hPCN plakin domain repeats 3-4<br /> | |||
[[5j1g]] – hPCN plakin domain repeats 7-8<br /> | |||
[[5j1f]], [[5j1h]] – hPCN plakin domain repeats 5-6<br /> | |||
[[5j1i]] – hPCN plakin domain repeats 7-9<br /> | |||
[[4gdo]] – hPCN rod domain<br /> | [[4gdo]] – hPCN rod domain<br /> | ||
[[3f7p]], [[4q58]] - hPCN actin-binding domain + integrin β4 residues 1126-1370<br /> | [[3f7p]], [[4q58]] - hPCN actin-binding domain + integrin β4 residues 1126-1370<br /> | ||
[[4q57]] - hPCN actin-binding domain + calmodulin N terminal<br /> | [[4q57]] - hPCN actin-binding domain + calmodulin N terminal<br /> | ||
[[2n03]] – hPCN C-terminal repeat domain 6 - NMR<br /> | |||
== References == | == References == | ||
<references/> | <references/> | ||
[[Category:Topic Page]] | [[Category:Topic Page]] | ||
Revision as of 13:34, 11 September 2017
<Structure load='1sh6' size='400' caption='Mouse plectin actin-binding domain 1sh6' scene= '>
FunctionFunction
Plectin, a universal and functionally versatile cytolinker protein, can be divided in three main sections; a central coiled-coil rod domain (residues 1492-1530), N and C-terminal globular region and exhibits a dumbbell like structure [1]. C-terminal region is composed of 6 homologous repeating domains (repeat#6 contains residues 4403-4606), and this region has a role in binding to intermediate filaments such as vimentin and cytokeratin[2], [3]. N-terminal globular region contains actin binding domain (ABD) (residues 175-400) comprising of two calponin homology (CH) domains, plakin domain (residues 300-1372) and N-terminal arm, which varies among isoforms.
For more details see Group:MUZIC:Plectin.
DiseaseDisease
Mutations in plectin result in skin fragility and blister formation[4].
3D structures of plectin3D structures of plectin
Updated on 11-September-2017
1mb8, 4q59 – hPCN actin-binding domain – human
1sh5, 1sh6 - PCN actin-binding domain – mouse
3pe0 - hPCN plakin domain residues 747-918
2odu, 2odv – hPCN plakin domain residues 300-530 (mutant)
3pdy – hPCN plakin domain repeats 3-4
5j1g – hPCN plakin domain repeats 7-8
5j1f, 5j1h – hPCN plakin domain repeats 5-6
5j1i – hPCN plakin domain repeats 7-9
4gdo – hPCN rod domain
3f7p, 4q58 - hPCN actin-binding domain + integrin β4 residues 1126-1370
4q57 - hPCN actin-binding domain + calmodulin N terminal
2n03 – hPCN C-terminal repeat domain 6 - NMR
ReferencesReferences
- ↑ Foisner R, Wiche G. Structure and hydrodynamic properties of plectin molecules. J Mol Biol. 1987 Dec 5;198(3):515-31. PMID:3430617
- ↑ Sutoh Yoneyama M, Hatakeyama S, Habuchi T, Inoue T, Nakamura T, Funyu T, Wiche G, Ohyama C, Tsuboi S. Vimentin intermediate filament and plectin provide a scaffold for invadopodia, facilitating cancer cell invasion and extravasation for metastasis. Eur J Cell Biol. 2014 Apr;93(4):157-69. doi: 10.1016/j.ejcb.2014.03.002. Epub, 2014 Apr 15. PMID:24810881 doi:http://dx.doi.org/10.1016/j.ejcb.2014.03.002
- ↑ Bouameur JE, Favre B, Fontao L, Lingasamy P, Begre N, Borradori L. Interaction of plectin with keratins 5 and 14: dependence on several plectin domains and keratin quaternary structure. J Invest Dermatol. 2014 Nov;134(11):2776-83. doi: 10.1038/jid.2014.255. Epub 2014, Jun 18. PMID:24940650 doi:http://dx.doi.org/10.1038/jid.2014.255
- ↑ Pfendner E, Rouan F, Uitto J. Progress in epidermolysis bullosa: the phenotypic spectrum of plectin mutations. Exp Dermatol. 2005 Apr;14(4):241-9. PMID:15810881 doi:http://dx.doi.org/10.1111/j.0906-6705.2005.00324.x