2e9i
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Solution structure of the N-terminal extended 20th Filamin domain from human Filamin-B
DiseaseDisease
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 StructureAbout this Structure
2E9I 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 17:07:44 2008
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OCACategories:
- Pages with broken file links
- 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