1x3b

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[[Image:1x3b.gif|left|200px]]
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{{Seed}}
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[[Image:1x3b.png|left|200px]]
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{{STRUCTURE_1x3b| PDB=1x3b | SCENE= }}
{{STRUCTURE_1x3b| PDB=1x3b | SCENE= }}
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'''Solution structure of the FAS1 domain of human transforming growth factor-beta induced protein IG-H3'''
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===Solution structure of the FAS1 domain of human transforming growth factor-beta induced protein IG-H3===
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==About this Structure==
==About this Structure==
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1X3B is a [[Single protein]] structure of 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=1X3B OCA].
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1X3B is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1X3B OCA].
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Rsgi]]
[[Category: Rsgi]]
[[Category: Structural genomic]]
[[Category: Structural genomic]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 14:28:26 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Sep 29 02:09:24 2008''

Revision as of 23:09, 28 September 2008

Image:1x3b.png

Template:STRUCTURE 1x3b

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 experimental information is available from OCA.

Page seeded by OCA on Mon Sep 29 02:09:24 2008

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OCA

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