1x3b
From Proteopedia
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
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
