3gef: Difference between revisions

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{{Seed}}
[[Image:3gef.png|left|200px]]
[[Image:3gef.jpg|left|200px]]


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{{STRUCTURE_3gef|  PDB=3gef  |  SCENE=  }}  
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===Crystal structure of the R482W mutant of lamin A/C===
===Crystal structure of the R482W mutant of lamin A/C===


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{{ABSTRACT_PUBMED_19574635}}


==About this Structure==
==About this Structure==
3GEF is a 4 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3GEF OCA].  
[[3gef]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3GEF OCA].  


==Reference==
==Reference==
<ref group="xtra">PMID:19574635</ref><references group="xtra"/>
<ref group="xtra">PMID:019574635</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Kozlov, S.]]
[[Category: Kozlov, S.]]
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[[Category: Wlodawer, A.]]
[[Category: Wlodawer, A.]]
[[Category: Zdanov, A.]]
[[Category: Zdanov, A.]]
[[Category: Acetylation]]
[[Category: Alternative splicing]]
[[Category: Cardiomyopathy]]
[[Category: Cardiomyopathy]]
[[Category: Charcot-marie-tooth disease]]
[[Category: Charcot-marie-tooth disease]]
[[Category: Coiled coil]]
[[Category: Disease mutation]]
[[Category: Disease mutation]]
[[Category: Immunoglobulin fold]]
[[Category: Immunoglobulin fold]]
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[[Category: Prenylation]]
[[Category: Prenylation]]
[[Category: Structural protein]]
[[Category: Structural protein]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug  5 10:24:07 2009''

Revision as of 17:26, 20 February 2013

File:3gef.png

Template:STRUCTURE 3gef

Crystal structure of the R482W mutant of lamin A/CCrystal structure of the R482W mutant of lamin A/C

Template:ABSTRACT PUBMED 19574635

About this StructureAbout this Structure

3gef is a 4 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

[xtra 1]

  1. Magracheva E, Kozlov S, Stewart CL, Wlodawer A, Zdanov A. Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD). Acta Crystallogr Sect F Struct Biol Cryst Commun. 2009 Jul 1;65(Pt, 7):665-70. Epub 2009 Jun 27. PMID:19574635 doi:10.1107/S1744309109020302

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