1x3b
From Proteopedia
(New page: 200px<br /> <applet load="1x3b" size="450" color="white" frame="true" align="right" spinBox="true" caption="1x3b" /> '''Solution structure of the FAS1 domain of hu...) |
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caption="1x3b" /> | caption="1x3b" /> | ||
'''Solution structure of the FAS1 domain of human transforming growth factor-beta induced protein IG-H3'''<br /> | '''Solution structure of the FAS1 domain of human transforming growth factor-beta induced protein IG-H3'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
- | 1X3B is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http:// | + | 1X3B is a [http://en.wikipedia.org/wiki/Single_protein 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]. |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: Kigawa, T.]] | [[Category: Kigawa, T.]] | ||
[[Category: Koshiba, S.]] | [[Category: Koshiba, S.]] | ||
- | [[Category: RSGI, RIKEN | + | [[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]] |
[[Category: Tochio, N.]] | [[Category: Tochio, N.]] | ||
[[Category: Tomizawa, T.]] | [[Category: Tomizawa, T.]] | ||
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[[Category: structural genomics ]] | [[Category: structural genomics ]] | ||
- | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:50:37 2008'' |
Revision as of 13:50, 21 February 2008
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Solution structure of the FAS1 domain of human transforming growth factor-beta induced protein IG-H3
Disease
Known diseases 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 Thu Feb 21 15:50:37 2008
Categories: Homo sapiens | Single protein | Inoue, M. | Kigawa, T. | Koshiba, S. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Tochio, N. | Tomizawa, T. | Yokoyama, S. | Yoneyama, M. | Beta ig-h3 | Cell adhesion protein | Extracellular matrix protein | Fas1 domain | Fasciclin | Integrin-interacting motif | National project on protein structural and functional analyses | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomics