2di8
From Proteopedia
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(New page: 200px<br /> <applet load="2di8" size="450" color="white" frame="true" align="right" spinBox="true" caption="2di8" /> '''Solution structure of the 19th filamin doma...)
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Revision as of 19:26, 12 November 2007
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Solution structure of the 19th 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
2DI8 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 21:32:58 2007
Categories: 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
