2ee9
From Proteopedia
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Solution structure of the 16th filamin domain from human Filamin-B
Disease
Known diseases associated with this structure: Atelosteogenesis, type III OMIM:[603381], Atelostogenesis, type I OMIM:[603381], Bare lymphocyte syndrome, type I OMIM:[170260], Boomerang dysplasia OMIM:[603381], Larson syndrome OMIM:[603381], Spondylocarpotarsal synostosis syndrome OMIM:[603381]
About this Structure
2EE9 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Feb 21 17:09:07 2008
Categories: Homo sapiens | Single protein | Harada, T. | Kigawa, T. | Koshiba, S. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Tomizawa, T. | Watanabe, S. | Yokoyama, S. | Beta-sandwich | Filamin | Immunoglobulin-like fold | National project on protein structural and functional analyses | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomics | Structural protein
