1x3b: Difference between revisions
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[[Image:1x3b.gif|left|200px]] | [[Image:1x3b.gif|left|200px]] | ||
'''Solution structure of the FAS1 domain of human transforming growth factor-beta induced protein IG-H3''' | {{Structure | ||
|PDB= 1x3b |SIZE=350|CAPTION= <scene name='initialview01'>1x3b</scene> | |||
|SITE= | |||
|LIGAND= | |||
|ACTIVITY= | |||
|GENE= TGFBI ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |||
}} | |||
'''Solution structure of the FAS1 domain of human transforming growth factor-beta induced protein IG-H3''' | |||
==Disease== | ==Disease== | ||
| Line 7: | Line 16: | ||
==About this Structure== | ==About this Structure== | ||
1X3B is a [ | 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]. | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
| Line 24: | Line 33: | ||
[[Category: fasciclin]] | [[Category: fasciclin]] | ||
[[Category: integrin-interacting motif]] | [[Category: integrin-interacting motif]] | ||
[[Category: national project on protein structural and functional | [[Category: national project on protein structural and functional analyse]] | ||
[[Category: nppsfa]] | [[Category: nppsfa]] | ||
[[Category: riken structural genomics/proteomics initiative]] | [[Category: riken structural genomics/proteomics initiative]] | ||
[[Category: rsgi]] | [[Category: rsgi]] | ||
[[Category: structural | [[Category: structural genomic]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:04:39 2008'' | ||
Revision as of 13:04, 20 March 2008
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| 1x3b | |||||||||||||
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| Gene: | TGFBI (Homo sapiens) | ||||||||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||||||||
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 Mar 20 15:04:39 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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 analyse
- Nppsfa
- Riken structural genomics/proteomics initiative
- Rsgi
- Structural genomic
