This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
1x5n
From Proteopedia
|
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
