2eea
From Proteopedia
Solution structure of the 17th filamin domain from human Filamin-B
Disease
Known disease associated with this structure: Atelosteogenesis, type III OMIM:[603381], Atelostogenesis, type I OMIM:[603381], Boomerang dysplasia OMIM:[603381], Larson syndrome OMIM:[603381], Spondylocarpotarsal synostosis syndrome OMIM:[603381]
About this Structure
2EEA 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 00:40:31 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 | Interaction with gp1ba | National project on protein structural and functional analyse | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomic | Structural protein
