2db9
From Proteopedia
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{{STRUCTURE_2db9| PDB=2db9 | SCENE= }} | {{STRUCTURE_2db9| PDB=2db9 | SCENE= }} | ||
- | + | ===Solution structure of the plus-3 domain of human KIAA0252 protein=== | |
+ | |||
+ | ==Disease== | ||
+ | Known disease associated with this structure: Congenital disorder of glycosylation, type In OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=611633 611633]] | ||
==About this Structure== | ==About this Structure== | ||
- | 2DB9 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full | + | 2DB9 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2DB9 OCA]. |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: Rsgi]] | [[Category: Rsgi]] | ||
[[Category: Structural genomic]] | [[Category: Structural genomic]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun | + | |
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Sep 28 17:38:59 2008'' |
Revision as of 14:39, 28 September 2008
Solution structure of the plus-3 domain of human KIAA0252 protein
Disease
Known disease associated with this structure: Congenital disorder of glycosylation, type In OMIM:[611633]
About this Structure
2DB9 is a Single protein structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Page seeded by OCA on Sun Sep 28 17:38:59 2008
Categories: Homo sapiens | Single protein | Inoue, M. | Kigawa, T. | Koshiba, S. | Nameki, N. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Tochio, N. | Yokoyama, S. | Yoneyama, M. | Kiaa0252 | National project on protein structural and functional analyse | Nppsfa | Plus-3 domain | Riken structural genomics/proteomics initiative | Rsgi | Structural genomic