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2dia

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|ACTIVITY=
|ACTIVITY=
|GENE= FLNB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= FLNB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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|DOMAIN=
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2dia FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2dia OCA], [http://www.ebi.ac.uk/pdbsum/2dia PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2dia RCSB]</span>
}}
}}
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==Disease==
==Disease==
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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]]
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Known disease 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]], 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 genomic]]
[[Category: structural genomic]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:27:29 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:35:00 2008''

Revision as of 23:35, 30 March 2008

Image:2dia.gif


PDB ID 2dia

Drag the structure with the mouse to rotate
Gene: FLNB (Homo sapiens)
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Solution structure of the 10th filamin domain from human Filamin-B


Disease

Known disease associated with this structure: Atelosteogenesis, type III OMIM:[603381], Atelostogenesis, type I OMIM:[603381], Boomerang dysplasia OMIM:[603381], Larson syndrome OMIM:[603381], Spondylocarpotarsal synostosis syndrome OMIM:[603381]

About this Structure

2DIA is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Mon Mar 31 02:35:00 2008

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