2di8 | pdb_00002di8
From Proteopedia
Solution structure of the 19th filamin domain from human Filamin-B
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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
2DI8 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 16:59:05 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Single protein
- Inoue, M.
- Kigawa, T.
- Koshiba, S.
- RSGI, RIKEN Structural Genomics/Proteomics Initiative.
- Tomizawa, T.
- Yokoyama, S.
- Beta-sandwich
- Filamin domain
- Immunoglobulin-like fold
- National project on protein structural and functional analyses
- Nppsfa
- Riken structural genomics/proteomics initiative
- Rsgi
- Structural genomics
