1x3b
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(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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Revision as of 17:51, 12 November 2007
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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 Mon Nov 12 19:58:06 2007
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
