1ufx
From Proteopedia
|
Solution structure of the third PDZ domain of human KIAA1526 protein
Disease
Known diseases associated with this structure: Deafness, autosomal recessive 31 OMIM:[607928], Usher syndrome, type IID OMIM:[607928]
About this Structure
1UFX 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 15:24:03 2008
Categories: Homo sapiens | Single protein | Aoki, M. | Hirota, H. | Inoue, M. | Kigawa, T. | Kikuno, R. | Kobayashi, N. | Koshiba, S. | Matsuda, T. | Matsuo, Y. | Nagase, T. | Nakayama, M. | Ohara, O. | Osanai, T. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Seki, E. | Shirouzu, M. | Tanaka, A. | Terada, T. | Tochio, N. | Yabuki, T. | Yokoyama, S. | Yoshida, M. | Pdz domain | Riken structural genomics/proteomics initiative | Rsgi | Structural genomics
