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1x3b
From Proteopedia
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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]) | ||
| + | |DOMAIN= | ||
| + | |RELATEDENTRY= | ||
| + | |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== | ||
| - | Known | + | 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]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''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
| |||||||
| 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
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 analyse | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomic
