1x5n
From Proteopedia
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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 Thu Feb 21 15:51:16 2008
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
