2ct2
From Proteopedia
Solution Structure of the RING domain of the Tripartite motif protein 32
Disease
Known disease associated with this structure: Bardet-Biedl syndrome 11 OMIM:[602290], Muscular dystrophy, limb-girdle, type 2H OMIM:[602290]
About this Structure
2CT2 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA. Page seeded by OCA on Sat May 3 22:59:31 2008
Categories: Homo sapiens | Single protein | Inoue, M. | Kigawa, T. | Koshiba, S. | Miyamoto, K. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Sato, M. | Tochio, N. | Yokoyama, S. | National project on protein structural and functional analyse | Nppsfa | Riken structural genomics/proteomics initiative | Ring domain | Rsgi | Structural genomic | Tat-interacting protein | Tripartite motif protein 32 | Zinc-finger protein ht2a
