2eed: Difference between revisions

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|ACTIVITY=  
|ACTIVITY=  
|GENE= FLNB, FLN1L, FLN3, TABP, TAP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= FLNB, FLN1L, FLN3, TABP, TAP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|DOMAIN=
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2eed FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2eed OCA], [http://www.ebi.ac.uk/pdbsum/2eed PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2eed RCSB]</span>
}}
}}


'''Solution structure of the 24th filamin domain from human Filamin-B'''
'''Solution structure of the 24th filamin domain from human Filamin-B'''


==Disease==
Known diseases associated with this structure: Atelosteogenesis, type III OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Atelostogenesis, type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Bare lymphocyte syndrome, type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170260 170260]], Boomerang dysplasia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Larson syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]], Spondylocarpotarsal synostosis syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603381 603381]]


==About this Structure==
==About this Structure==
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[[Category: structural protein]]
[[Category: structural protein]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:39:04 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:47:50 2008''
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