1x3b

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|ACTIVITY=
|ACTIVITY=
|GENE= TGFBI ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= TGFBI ([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=1x3b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1x3b OCA], [http://www.ebi.ac.uk/pdbsum/1x3b PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1x3b RCSB]</span>
}}
}}
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==Disease==
==Disease==
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Known diseases associated with this structure: Corneal dystrophy, Avellino type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, Groenouw type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, Reis-Bucklers type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, Thiel-Behnke type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, epithelial basement membrane OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, lattice type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, lattice type IIIA OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]]
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Known disease associated with this structure: Corneal dystrophy, Avellino type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, Groenouw type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, Reis-Bucklers type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, Thiel-Behnke type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, epithelial basement membrane OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, lattice type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]], Corneal dystrophy, lattice type IIIA OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692 601692]]
==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 15:04:39 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:44:20 2008''

Revision as of 21:44, 30 March 2008

Image:1x3b.gif


PDB ID 1x3b

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



Solution structure of the FAS1 domain of human transforming growth factor-beta induced protein IG-H3


Disease

Known disease associated with this structure: Corneal dystrophy, Avellino type OMIM:[601692], Corneal dystrophy, Groenouw type I OMIM:[601692], Corneal dystrophy, Reis-Bucklers type OMIM:[601692], Corneal dystrophy, Thiel-Behnke type OMIM:[601692], Corneal dystrophy, epithelial basement membrane OMIM:[601692], Corneal dystrophy, lattice type I OMIM:[601692], Corneal dystrophy, lattice type IIIA OMIM:[601692]

About this Structure

1X3B 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 00:44:20 2008

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OCA

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