2eea | pdb_00002eea
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 crystallographic information is available from OCA. Page seeded by OCA on Sun May 4 02:25:06 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- 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
- Interaction with gp1ba
- National project on protein structural and functional analyse
- Nppsfa
- Riken structural genomics/proteomics initiative
- Rsgi
- Structural genomic
- Structural protein
