1x5n
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(New page: 200px<br /> <applet load="1x5n" size="450" color="white" frame="true" align="right" spinBox="true" caption="1x5n" /> '''Solution structure of the second PDZ domain...)
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Revision as of 17:53, 12 November 2007
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Solution structure of the second PDZ domain of harmonin protein
Disease
Known diseases associated with this structure: Deafness, autosomal recessive 18 OMIM:[605242], Usher syndrome, type 1C OMIM:[605242]
About this Structure
1X5N 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 20:00:07 2007
Categories: Homo sapiens | Single protein | Hayashi, F. | Qin, X.R. | RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative. | Yokoyama, S. | Antigen ny-co-38/ny-co-37 | Autoimmune enteropathy-related antigen aie-75 | Harmonin | National project on protein structural and functional analyses | Nppsfa | Pdz domain | Pdz-73 protein | Riken structural genomics/proteomics initiative | Rsgi | Structural genomics | Usher syndrome 1c protein
