1x3b
From Proteopedia
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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
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
